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CA2500964A1 - Cyclohexyl sulphone derivatives as gamma-secretase inhibitors - Google Patents

Cyclohexyl sulphone derivatives as gamma-secretase inhibitors Download PDF

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Publication number
CA2500964A1
CA2500964A1 CA002500964A CA2500964A CA2500964A1 CA 2500964 A1 CA2500964 A1 CA 2500964A1 CA 002500964 A CA002500964 A CA 002500964A CA 2500964 A CA2500964 A CA 2500964A CA 2500964 A1 CA2500964 A1 CA 2500964A1
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Prior art keywords
6alkyl
halogen
compound according
ocor3a
co2r3
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CA002500964A
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French (fr)
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CA2500964C (en
Inventor
Ian Churcher
Timothy Harrison
Sonia Kerrad
Paul Joseph Oakley
Duncan Edward Shaw
Martin Richard Teall
Susannah Williams
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Organon Pharma UK Ltd
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    • C07C2601/12—Systems containing only non-condensed rings with a six-membered ring
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Abstract

Compounds of formula (I) inhibit the processing of APP by gamma-secretase, and hence are useful in treatment of Alzheimer's disease.

Claims (10)

1. A compound of formula I:
wherein X represents SCN, SR1, S(O)R1, (CR a R b)m SO2R1, SO2N(R2)2, SO2NHCOR1, SO2NHN(R2)2, OSO2N(R2)2, OS(O)N(R2)2, OSO2NHCOR1, COR4, NHCOR1, NHCO2R1, NHCON(R2)2, NHSO2R1 or NHSO2N(R2)2;
m is 0 or 1 R a represents H or C1-4alkyl;
R b represents H, C1-4alkyl, CO2H, C1-4alkoxycarbonyl or C1-4alkylsulphonyl; or R b may combine with R1 to form a 5- or 6-membered ring;
L represents a bond, =CH- or -(CHR a)n-; with the proviso that L
does not represent a bond when X represents NHCOR1, NHCO2R1 or NHSO2R1; and with the proviso that if L represents =CH-, X represents SO2R1 or COR4;
n is 1, 2 or 3;
R1 represents CF3 or C1-6alkyl, C2-6alkenyl, C3-9cycloalkyl or C3-6cycloalkylC1-6alkyl, any of which may bear up to 2 substituents selected from halogen, CN, CF3, OR3, COR3, CO2R3, OCOR3a, SO2R3a, N(R5)2, and CON(R5)2, or R1 represents aryl, arylC1-6alkyl, C-heterocyclyl or C-heterocyclylC1-6alkyl;
or R1 may combine with R b to form a 5- or 6-membered ring;
each R2 independently represents H, C1-6alkoxy, or C1-6alkyl, C2-6alkenyl, C3-9cycloalkyl or C3-6cycloalkylC1-6alkyl, any of which may bear up to 2 substituents selected from halogen, CN, CF3, OR3, COR3, CO2R3, OCOR3a, and CON(R5)2; or aryl, arylC1-6alkyl, C-heterocyclyl or C-heterocyclylC1-6alkyl;
or two R2 groups together with a nitrogen atom to which they are mutually attached complete an N-heterocyclyl group R3 represents H, C1-4alkyl, phenyl or heteroaryl;
R3a represents C1-4alkyl, phenyl or heteroaryl;
R4 represents (CR a R b)SO2R1, pyridine N-oxide, or phenyl or heteroaryl which bear a substituent selected from CO2H, methylenedioxy, difluoromethylenedioxy, COR3, C-heterocyclyl, C1-4alkylsulphonyl and substituted C1-6alkyl, C1-6alkoxy, C2-6alkenyl or C2-6alkenyloxy wherein the substituent is selected from halogen, CN, CF3, OR3, CO2R3, OCOR3a, N(R5)2 and CON(R5)2;
R5 represents H or C1-4alkyl, or two R5 groups together with a nitrogen atom to which they are mutually attached complete an azetidine, pyrrolidine, piperidine, morpholine, thiomorpholine or thiomorpholine-1,1-dioxide ring;
Ar1 and Ar2 independently represent phenyl or heteroaryl, either of which bears 0-3 substituents independently selected from halogen, CN, NO2, CF3, CHF2, OH, OCF3, CHO, CH=NOH, C1-4alkoxy, C1-4alkoxycarbonyl, C2-6acyl, C2-6alkenyl and C1-4alkyl which optionally bears a substituent selected from halogen, CN, NO2, CF3, OH and C1-4alkoxy;
"aryl" at every occurrence thereof refers to phenyl or heteroaryl which optionally bear up to 3 substituents selected from halogen, CN, NO2, CF3, OCF3, OR3, COR3, CO2R3, OCOR3a, N(R5)2, CON(R5)2 and optionally-substituted C1-6alkyl, C1-6alkoxy, C2-6alkenyl or C2-6alkenyloxy wherein the substituent is selected from halogen, CN, CF3, phenyl, OR3, CO2R3, OCOR3a, N(R5)2 and CON(R5)2; and "C-heterocyclyl" and "N-heterocyclyl" at every occurrence thereof refer respectively to a heterocyclic ring system bonded through carbon or nitrogen, said ring system being non-aromatic and comprising up to 10 atoms, at least one of which is O, N or S, and optionally bearing up to 3 substituents selected from oxo, halogen, CN, NO2, CF3, OCF3, OR3, COR3, CO2R3, OCOR3a, OSO2R3a, N(R5)2, CON(R5)2 and optionally-substituted phenyl, C1-6alkyl, C1-6alkoxy, C2-6alkenyl or C2-6alkenyloxy wherein the substituent is selected from halogen, CN, CF3, OR3, CO2R3, OCOR3a, N(R5)2 and CON(R5)2;
or a pharmaceutically acceptable salt thereof.
2. A compound according to claim 1 wherein X is selected from SR1, (CR a R b)m SO2R1, SO2N(R2)2, OSO2N(R2)2, COR4, NHCOR1, NHCO2R1, NHCON(R2)2, NHSO2R1 and NHSO2N(R2)2.
3. A compound according to claim 1 which is in accordance with formula II:
or a pharmaceutically acceptable salt thereof.
4. A compound according to claim 1 which is in accordance with formula II:
wherein p is 0, 1, 2 or 3;

Y is SCN, SR1, S(O)R1, (CR a R b)m SO2R1, SO2N(R2)2, SO2NHCOR1, SO2NHN(R2)2, OSO2N(R2)2, OS(O)N(R2)2, OSO2NHCOR1, COR4, NHCON(R2)2 or NHSO2N(R2)2;
and m, R a, R b, R1, R2, R4, Ar1 and Ar2 are as defined in claim 1;
or a pharmaceutically acceptable salt thereof.
5. A compound according to claim 1 which is in accordance with formula IV:
wherein Z represents SO2R1 or COR4;
and R1, R4, Ar1 and Ar2 are as defined in claim 1;
or a pharmaceutically acceptable salt thereof.
6. A compound according to any previous claim wherein Ar1 is 4-chlorophenyl or 4-trifluoromethylphenyl or 6-(trifluoromethyl)-3-pyridyl and Ar2 is 2,5-difluorophenyl.
7. A pharmaceutical composition comprising a compound according to any previous claim and a pharmaceutically acceptable carrier.
8. A compound according to any of claims 1-6 for use in a method of treatment of the human body.
9. The use of a compound according to any of claims 1-6 in the manufacture of a medicament for treating or preventing Alzheimer's disease.
10. A method of treatment of a subject suffering from or prone to a condition associated with the deposition of .beta.-amyloid which comprises administering to that subject an effective amount of a compound according to any of claims 1-6.
CA2500964A 2002-10-04 2003-09-25 Cyclohexyl sulphone derivatives as gamma-secretase inhibitors Expired - Fee Related CA2500964C (en)

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